Cargando…

Investigating Colorimetric Protein Array Assay Schemes for Detection of Recurrence of Bladder Cancer

A colorimetric microarray for the multiplexed detection of recurrence of bladder cancer including protein markers interleukin-8 (IL8), decorin (DCN), and vascular endothelial growth factor (VEGF) was established to enable easy and cheap read-out by a simple office scanner paving the way for quick th...

Descripción completa

Detalles Bibliográficos
Autores principales: Gogalic, Selma, Sauer, Ursula, Doppler, Sara, Preininger, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5872058/
https://www.ncbi.nlm.nih.gov/pubmed/29364182
http://dx.doi.org/10.3390/bios8010010
_version_ 1783309753973211136
author Gogalic, Selma
Sauer, Ursula
Doppler, Sara
Preininger, Claudia
author_facet Gogalic, Selma
Sauer, Ursula
Doppler, Sara
Preininger, Claudia
author_sort Gogalic, Selma
collection PubMed
description A colorimetric microarray for the multiplexed detection of recurrence of bladder cancer including protein markers interleukin-8 (IL8), decorin (DCN), and vascular endothelial growth factor (VEGF) was established to enable easy and cheap read-out by a simple office scanner paving the way for quick therapy monitoring at doctors’ offices. The chip is based on the principle of a sandwich immunoassay and was optimized prior to multiplexing using IL8 as a model marker. Six different colorimetric assay formats were evaluated using a detection antibody (dAB) labeled with (I) gold (Au) nanoparticles (NPs), (II) carbon NPs, (III) oxidized carbon NPs, and a biotinylated dAB in combination with (IV) neutravidin–carbon, (V) streptavidin (strp)–gold, and (VI) strp–horseradish peroxidase (HRP). Assay Format (III) worked best for NP-based detection and showed a low background while the enzymatic approach, using 3,3′,5,5′-tetramethylbenzidine (TMB) substrate, led to the most intense signals with good reproducibility. Both assay formats showed consistent spot morphology as well as detection limits lower than 15 ng/L IL8 and were thus applied for the multiplexed detection of IL8, DCN, and VEGF in synthetic urine. Colorimetric detection in urine (1:3) yields reaction signals and measurement ranges well comparable with detection in the assay buffer, as well as excellent data reproducibility as indicated by the coefficient of variation (CV 5–9%).
format Online
Article
Text
id pubmed-5872058
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-58720582018-03-29 Investigating Colorimetric Protein Array Assay Schemes for Detection of Recurrence of Bladder Cancer Gogalic, Selma Sauer, Ursula Doppler, Sara Preininger, Claudia Biosensors (Basel) Article A colorimetric microarray for the multiplexed detection of recurrence of bladder cancer including protein markers interleukin-8 (IL8), decorin (DCN), and vascular endothelial growth factor (VEGF) was established to enable easy and cheap read-out by a simple office scanner paving the way for quick therapy monitoring at doctors’ offices. The chip is based on the principle of a sandwich immunoassay and was optimized prior to multiplexing using IL8 as a model marker. Six different colorimetric assay formats were evaluated using a detection antibody (dAB) labeled with (I) gold (Au) nanoparticles (NPs), (II) carbon NPs, (III) oxidized carbon NPs, and a biotinylated dAB in combination with (IV) neutravidin–carbon, (V) streptavidin (strp)–gold, and (VI) strp–horseradish peroxidase (HRP). Assay Format (III) worked best for NP-based detection and showed a low background while the enzymatic approach, using 3,3′,5,5′-tetramethylbenzidine (TMB) substrate, led to the most intense signals with good reproducibility. Both assay formats showed consistent spot morphology as well as detection limits lower than 15 ng/L IL8 and were thus applied for the multiplexed detection of IL8, DCN, and VEGF in synthetic urine. Colorimetric detection in urine (1:3) yields reaction signals and measurement ranges well comparable with detection in the assay buffer, as well as excellent data reproducibility as indicated by the coefficient of variation (CV 5–9%). MDPI 2018-01-24 /pmc/articles/PMC5872058/ /pubmed/29364182 http://dx.doi.org/10.3390/bios8010010 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gogalic, Selma
Sauer, Ursula
Doppler, Sara
Preininger, Claudia
Investigating Colorimetric Protein Array Assay Schemes for Detection of Recurrence of Bladder Cancer
title Investigating Colorimetric Protein Array Assay Schemes for Detection of Recurrence of Bladder Cancer
title_full Investigating Colorimetric Protein Array Assay Schemes for Detection of Recurrence of Bladder Cancer
title_fullStr Investigating Colorimetric Protein Array Assay Schemes for Detection of Recurrence of Bladder Cancer
title_full_unstemmed Investigating Colorimetric Protein Array Assay Schemes for Detection of Recurrence of Bladder Cancer
title_short Investigating Colorimetric Protein Array Assay Schemes for Detection of Recurrence of Bladder Cancer
title_sort investigating colorimetric protein array assay schemes for detection of recurrence of bladder cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5872058/
https://www.ncbi.nlm.nih.gov/pubmed/29364182
http://dx.doi.org/10.3390/bios8010010
work_keys_str_mv AT gogalicselma investigatingcolorimetricproteinarrayassayschemesfordetectionofrecurrenceofbladdercancer
AT sauerursula investigatingcolorimetricproteinarrayassayschemesfordetectionofrecurrenceofbladdercancer
AT dopplersara investigatingcolorimetricproteinarrayassayschemesfordetectionofrecurrenceofbladdercancer
AT preiningerclaudia investigatingcolorimetricproteinarrayassayschemesfordetectionofrecurrenceofbladdercancer